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. 2002 Feb;127(2):234–242. doi: 10.1046/j.1365-2249.2002.01767.x

Fig. 1.

Fig. 1

Schematic representation of the HAV genome and ssRNA constructs used for transfection. Restriction enzyme sites within the full-length cDNA construct pHAV38-2 [19,20] are shown. In vitro transcription following digestion with HaeII yields full-length RNA (full), whereas XhoI or EcoRI yields truncated RNAs (ΔX and ΔE, respectively) that do not contain the region essential for RNA-dependent RNA synthesis [19,20].